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(Displays ligands and other sites on GSK-3 beta.) |
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1. Difference that can be observed from complexes of Staurosporine with GSK-3 beta and other protein kinases such as CDK2, Chk1, Lck and PKA | 1. Difference that can be observed from complexes of Staurosporine with GSK-3 beta and other protein kinases such as CDK2, Chk1, Lck and PKA | ||
| - | + | In GSK-3 beta complex with Staurosporine, water is a part of a hydrogen-bonding network | |
| - | + | 2. Difference that can be observed from GSK-3 beta complexes with Staurosporine and other inhibitors (AMP-PNP, indirubin-3'-monoxime) | |
| - | + | Between GSK-3 beta complex with Stauroporine and AMP-PNP, the position of N-terminal domain varies. | |
| - | - The angles of binding in the active site are different | ||
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| - | - Between GSK-3 beta complex with Stauroporine and AMP-PNP, the position of N-terminal domain varies | ||
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| - | - In GSK-3 beta complex with indirubin-3'-monoxime, water is also a part of hydrogen bond, which is observed in complex with Stauroporine | ||
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<scene name='48/483890/Gsk-3_beta_with_staurosporine/1'>GSK-3 beta complex with Staurosporine</scene> | <scene name='48/483890/Gsk-3_beta_with_staurosporine/1'>GSK-3 beta complex with Staurosporine</scene> | ||
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| - | + | http://upload.wikimedia.org/wikipedia/commons/3/34/Staurosporine1.png | |
| - | <scene name='48/483890/Nerses/1'> | + | <scene name='48/483890/Nerses/1'>Display Bonding Preferences (Focus on Red)</scene> |
==Quiz Question 2== | ==Quiz Question 2== | ||
Revision as of 05:03, 13 March 2015
| This Sandbox is Reserved from January 19, 2016, through August 31, 2016 for use for Proteopedia Team Projects by the class Chemistry 423 Biochemistry for Chemists taught by Lynmarie K Thompson at University of Massachusetts Amherst, USA. This reservation includes Sandbox Reserved 425 through Sandbox Reserved 439. |
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